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nsv5541234

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:398,193

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1470 SVs from 81 studies. See in: genome view    
Submitted genomic35,873,808-36,272,000Question Mark
Overlapping variant regions from other studies: 1470 SVs from 81 studies. See in: genome view    
Remapped(Score: Perfect):37,246,106-37,644,298Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5541234Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000021.9Chr2135,873,80836,272,000
nsv5541234RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000021.8Chr2137,246,10637,644,298

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17726725duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17726725Submitted genomicNC_000021.9:g.3587
3808_36272000dup
GRCh38 (hg38)NC_000021.9Chr2135,873,80836,272,000
nssv17726725RemappedPerfectNC_000021.8:g.3724
6106_37644298dup
GRCh37.p13First PassNC_000021.8Chr2137,246,10637,644,298

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv17726725<0.00116404
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